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Nitani, Noriko; Kuramoto, Kenichi; Yamashita, Toshiyuki; Omichi, Toshihiko*
Progress in Nuclear Energy, 38(3-4), p.435 - 438, 2001/02
Times Cited Count:1 Percentile:11.99(Nuclear Science & Technology)no abstracts in English
*; Sato, Haruo; *
JNC TN8400 99-059, 59 Pages, 1999/10
Organic acids in groundwater are considered to form complexes and increase the solubility of radionuclides released from vitrified waste in a high-level radioactive waste (HLW) repository. To ivestigate whether the solubility of samarium (Sm) is influenced by organic substances, we measured Sm solubility in the presence of different organic substances and compared those values with results from thermodynamic predictions. Humic acid (Aldrich) is commercially available and soluble organic matter originated from bentonite were used as organic substances in this study. Consequently, the solubility of Sm showed a tendency to apparently increase with icreasing the concentration of humic acid, but in the presence of carbonate, thermodynamic predictions suggested that the dominant species are carbonate complexes and that the effect of organic substances are less than that of carbonate. Based on total organic carbon (TOC), the increase of Sm solubility measured with humic acid (Aldrich) was more significant than that in the case with soluble organic matter originated from bentonite. Since bentonite is presumed to include also simple organic matters of which stability constant for forming complexes is low, the effect of soluble organic matter originated from bentonite on the solubility of Sm is eonsidered to be less effective than that of humic acid (Aldrieh). Experimental values were compared with model prediction, propsed by Kim, based on data measured in a low pH region. Tentatively we calculated the increase in Sm solubility assuming complexation with humic acid. Trial calculations were carried out on the premise that the complexation reaction of metal ion with humic acid is based on neutralization process by 1-1 complexation. In this process, it was assumed that one metal ion coordinates with one unit of complexation sites which number of proton exchange sites is equal to ionic charge. Consequently, Kim's model indicated that carbonate complexes should be dominant ...
Kobayashi, Yutaro*; Haga, Kazuko*; Kaneda, Yoshihisa*; Sato, Tsutomu*; Kakuda, Ayaka; Osugi, Takeshi; Sone, Tomoyuki; Kuroki, Ryoichiro
no journal, ,
no abstracts in English